Entity Details

Primary name LIM2
Entity type gene
Source Source Link

Details

PrimaryID3982
RefseqGeneNG_012924
SymbolLIM2
Namelens intrinsic membrane protein 2
Chromosome19
Location19q13.41
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-21
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsLMIP_HUMAN

GO terms

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GOName
GO:0002088 lens development in camera-type eye
GO:0005212 structural constituent of eye lens
GO:0005886 plasma membrane
GO:0007043 cell-cell junction assembly
GO:0016021 integral component of membrane
GO:0030054 cell junction
GO:0031982 vesicle

Diseases

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Disease IDSourceNameDescription
615277 OMIMCataract, multiple types 19 (CTRCT19)An opacification of the crystalline lens of the eye that frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. The disease is caused by variants affecting the gene represented in this entry.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
LIM2LGALS3HPRD11532191 details
LIM2ACTA2BioGRID, IntAct28514442 details